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1.
Journal of Veterinary Science ; : 257-262, 2013.
Article Dans Anglais | WPRIM | ID: wpr-92906

Résumé

Vitamin D3 up-regulated protein 1 (VDUP1) is a potent growth suppressor that inhibits tumor cell proliferation and cell cycle progression when overexpressed. In a previous study, we showed that VDUP1 knockout (KO) mice exhibited accelerated liver regeneration because such animals could effectively control the expression of cell cycle regulators that drive the G1-to-S phase progression. In the present study, we further investigated the role played by VDUP1 in initial priming of liver regeneration. To accomplish this, VDUP1 KO and wild-type (WT) mice were subjected to 70% partial hepatectomy (PH) and sacrificed at different times after surgery. The hepatic levels of TNF-alpha and IL-6 increased after PH, but there were no significant differences between VDUP1 KO and WT mice. Nuclear factor-kappaB (NF-kappaB), c-Jun-N-terminal kinase (JNK), and signal transducer and activator of transcription 3 (STAT-3) were activated much earlier and to a greater extent in VDUP1 KO mice after PH. A single injection of TNF-alpha or IL-6 caused rapid activation of JNK and STAT-3 expression in both mice, but the responses were stronger and more sustained in VDUP1 KO mice. In conclusion, our findings provide evidence that VDUP1 plays a role in initiation of liver regeneration.


Sujets)
Animaux , Mâle , Technique de Western , Protéines de transport/génétique , Prolifération cellulaire , Régulation de l'expression des gènes , Hépatectomie , Hépatocytes/cytologie , JNK Mitogen-Activated Protein Kinases/génétique , Foie/physiologie , Souris knockout , Facteur de transcription NF-kappa B/génétique , Réaction de polymérisation en chaîne , Régénération , Facteur de transcription STAT-3/génétique , Thiorédoxines/génétique
2.
Rev. colomb. psiquiatr ; 41(1): 217-228, ene.-abr. 2012. ilus, graf, tab
Article Dans Espagnol | LILACS | ID: lil-639942

Résumé

Introducción: En psiquiatría de enlace se logra obtener una visión integral del tratamiento y de las necesidades de cada paciente prestando especial atención a las interacciones medicamentosas y a las contraindicaciones. Algunos casos particulares motivaron la descripción, reporte y revisión bibliográfica acerca de otras posibles aplicaciones de fármacos antagonistas de los recetores 5HT2A y 3, particularmente mirtazapina y olanzapina, en síndrome de hiperalgesia, tinitus y leucoencefalopatía multifocal progresiva por virus JC. Método: reporte de casos. Resultados y Conclusiones: Se describen los casos de tres pacientes en los cuales fue necesario usar mirtazapina y olanzapina no solo para el control de los síntomas psiquiátricos (afectivos, comportamentales y trastorno del sueño), sino también como coadyuvantes en las patologías de base de cada paciente. El uso de cualquier medicamento en psiquiatría de enlace debe tener en cuenta el contexto del paciente, la comorbilidad, las contraindicaciones y las interacciones farmacológicas para garantizar un desenlace positivo, además de promover el trabajo multidisciplinario entre especialistas.


Introduction: In liaison psychiatry it is possible to get an integral view of patient's treatment and needs, paying special attention to pharmacological interactions and contraindications. Some particular cases motivated the description, report and review about other possible applications of 5HT2A and 5HT3 antagonist, particularly Mirtazapine and Olanzapine, in hyperalgesia syndrome, tinnitus and Progressive Multifocal Leukoencephalopathy by JC virus. Method: Cases report. Results: We describe 3 cases of patients in which Mirtazapine and Olanzapine were necessary not only to control psychiatric symptoms (affective / behavioral symptoms and insomnia) but to act as adjuvant therapy in axis III diseases. The use of any drug in psychiatry must take in to account the context of the patient, the presence of comorbidity, contraindications and pharmacological interactions so as to grant a positive outcome also promoting the multidisciplinary work between specialists.


Sujets)
Humains , Protéines adaptatrices de la transduction du signal/métabolisme , Noyau de la cellule/métabolisme , Cystéine/métabolisme , Neurones/métabolisme , Thiorédoxines/métabolisme , Facteurs de transcription/métabolisme , Motifs d'acides aminés , Protéines adaptatrices de la transduction du signal/génétique , Lignée cellulaire tumorale , Cystéine/composition chimique , Cytoplasme/métabolisme , Disulfures/composition chimique , Analyse de profil d'expression de gènes , Régulation de l'expression des gènes , Annotation de séquence moléculaire , Données de séquences moléculaires , Mutation , Neurones/cytologie , Oxydoréduction , Cartographie d'interactions entre protéines , Transduction du signal , Transcription génétique , Thiorédoxines/génétique , Facteurs de transcription/génétique
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